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Mitochondrial genetic diseases
PURPOSE OF REVIEW: Mitochondrial diseases are individually uncommon, but collectively pose a significant burden on human health. Primary mitochondrial disease is caused by defects in the mitochondrial DNA-encoded genes or in nuclear genes whose products are imported into the mitochondrion. Great str...
Tallennettuna:
| Päätekijät: | , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2010
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3586258/ https://ncbi.nlm.nih.gov/pubmed/21045694 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MOP.0b013e3283402e21 |
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